Influence of plasticizer on ionic conductivity of PVC-PBMA polymer electrolytes

Plasticized polymer electrolytes comprising of ethylene carbonate as the plasticizing agent in poly (vinyl chloride) [PVC]–poly (butyl methacrylate) [PBMA] blended polymer electrolytes were prepared by solution casting technique. Complex formation, structural elucidation, conductivity, dielectric parameters (?′, ?″, M′, and M″), thermal stability, and surface morphology are brought out from FTIR, XRD, ac impedance analysis, dielectric studies, thermogravimetry/differential thermal analysis, and scanning electron microscopic studies, respectively. Polymer electrolytes are found to exhibit higher ionic conductivity at higher concentration of plasticizer at the cost of their mechanical stability. Conductivity of 1.879 × 10^?4 S cm^?1 is exhibited by the polymer electrolyte consisting of 69% of plasticizer with appreciable thermal stability up to 523 K. Temperature and frequency dependence of conductivity is found to follow Vogel Tammann Fulcher relation and Jonscher power law, respectively. Real and imaginary parts of dielectric constants are found to decrease with increase in frequency which could be due to the electrode polarization effect.     

FTIR reflectance studies of electrochemically prepared polypyrrole films

-1 . The effects of some relevant electrochemical parameters (the electrolyte, the polymerization current density, and the deposition time) on the reflectance spectra of polypyrrole are reported. The optical constants for polypyrrole films were calculated from the reflectance spectra by Kramers–Kronig technique. The decrease of the electropolymerization current density and film thickness results in an increase of the reflectance and dc conductivity values for PPY(TSO). Received: 6 November 1997/Accepted: 17 December 1997     

Influence of sputtering conditions on ionic conductivity of LiPON thin films

LiPON films were deposited using radio-frequency magnetron sputtering in a pure N₂ gas atmosphere. The influence of rf power, N₂ pressure, target–substrate distance and target density on thin film composition and ionic conductivity has been studied. Impedance measurements performed between 25 and 80 °C have indicated that ionic conductivity increases with nitrogen incorporation into the glass structure. An increase in the deposition rate with the target density has also been observed.     

Electrical conductivity of individual polypyrrole microtube

Conducting microtubes (0.4－0.5μm in outer diameter) made of polypyrrole (PPy) doped with p-toluene sulfonic acid (PTSA) were synthesized by a self-assembly method. We report the electrical conductivity of an individual PPy microtube, on which a pair of platinum micro-leads was fabricated by focused ion beam deposition. The measured room-temperature conductivity of the individual PPy microtube was 0.29S/cm, which is comparable to that of template-synthesized PPy micro/nanotubes. The temperature dependence of conductivity of the individual microtube follows the three-dimensional variable-range hopping (3D VRH) model.     

Influence of acceptor doping on ionic conductivity in alkali earth titanate perovskites

The electrical conductivity of the SrTi_1−xFe_xO_3−δ, BaTi_1−xFe_xO_3−δ and SrTi_1−xMn_xO_3−δ systems has been studied in a range of oxygen partial pressures between 10⁻¹⁶ and 0.21 atm at 900 and 1000 °C. The materials exhibit predominantly ionic conductivity in a wide range of intermediate oxygen partial pressures. It has been found that in Fe doped strontium and barium titanates, the dependencies of the ionic conductivity on the acceptor concentration show a local maximum near x=0.2. Taking into account that in the CaTi_1−xFe_xO_3−δ system (x=0−0.5), the concentration dependence of the ionic conductivity also has a maximum near x=0.2, it can be concluded that this is a common phenomenon for Fe doped alkali earth titanates. An assumption has been made that a scheme of defect formation devised earlier for Fe doped calcium titanate is applicable for other alkali earth titanates.     

Influence of grain sizes on the ionic conductivity and the chemical diffusion coefficient in copper selenide

Ionic conductivity and chemical diffusion coefficient have been studied for superionic polycrystalline Cu_1.75Se copper selenide within the temperature interval 300–500 K. An increase in ionic conductivity with an grain size increase is observed. In our opinion, this fact is caused by lower activation energy for the bulk diffusion than that for the grain boundary diffusion.     

Influence of calcium substitution on the phase transition and ionic conductivity in BICAVOX oxide ion conductor

Samples of Bi₄Ca _x V_{2? x} O_{11?(3 x /2)?δ} in the composition range 0.07 ≤ x ≤ 0.30 were prepared by conventional solid state reactions. The stability of different phases as a function of composition was analysed by X-ray powder diffraction, FT-IR spectra, differential thermal analysis and AC impedance spectroscopy. For the compositions x ≤ 0.10, monoclinic α-phase structure is retained at room temperature. For x = 0.13, orthorhombic β-phase is observed, whereas for x ≥ 0.17, high O^2?conducting tetragonal γ-phase is stabilised. However, the highest ionic conductivity σ_300°C = 3.27 × 10^?4 S cm^?1 was observed for x = 0.17. This higher value of conductivity of the substituted compound as compared to the parent compound can be attributed to the increased oxygen ion vacancies generated as a result of cation doping. AC impedance spectroscopy reveals the fact that this ionic conductivity is mainly due to the grain contribution.     

Increasing the crystallite and conductivity of polypyrrole with dopant used

The chemical polymerization method is very convenient for obtaining a plurality of the polymer. Chemical synthesizes of polypyrrole (PPy) were performed in acetonitrile solutions containing different dopants: dodecylbenzene sulphonic acid (DBSA), tetrafluoroborate (BF₄ ^?), perchlorate (ClO₄ ^?) and oxalate (C₂O₄ ^2?). These polymers were characterized by using scanning electron microscopy (SEM), ultraviolet–visible (UV–Vis) spectrophotometer, Fourier transform infrared spectrometry (FTIR), X-ray diffraction (XRD) techniques and dry conducting measurement. It was observed that the interactions between the polymers and dopant materials are completely different from each other. As a result of this interaction, the conductivities and crystal structures of PPy are also different from each other. Results in this work showed that the dopants used affected both electrical conductivities and crystal structures of PPy.     

On the ionic conductivity of anion-doped sodium Chloride

Abstract

Isotherms showing the dependence of the conductivity of NaCl crystals on the concentration c_x of S^2- ions have revealed that the values of c_x determined by least-squares fitting of the conductivity ([sgrave]) data are not mutually consistent.     

Luminescence and ionic conductivity of bariumfluorochloride

The luminescence and ionic conductivity of pure and doped BaFCl crystals are reported. The ionic conductivity occurs mainly via chloride ion vacancies, whereas the efficient, yellow luminescence is ascribed to oxygen impurities (O′_F).     

Influence of optical-damage-resistant dopants on the nonlinear optical properties of lithium niobate

Using the chemical-bond method, nonlinear optical properties of lithium niobate containing different dopants are calculated. In crystals with stoichiometric composition the second order nonlinear susceptibility decreases approximately linearly with increasing dopant concentration. Among the dopants studied – Mg, Zn and In – this behaviour is most highly expressed for In doping. In contrast to that, congruently grown crystals show a different behaviour; only a weak dependence on the dopant concentration is found for, for example, Mg-doped material. Received: 24 October 2000 / Published online: 21 March 2001     

Determining ionic conductivity from structural models of fast ionic conductors

Reverse Monte Carlo produced structural models of silver ion conducting glasses and crystals have been investigated by the bond-valence technique. Both absolute ionic conductivity and activation energy can be determined directly from the "pathway volume" of the structural models, i.e., from the volume fraction of the percolating pathway cluster. This pathway volume-conductivity relation was found to hold for glassy and crystalline systems with silver ion conductivities differing by more than 11 orders of magnitude. Earlier, less universal rules were rationalized and unified by means of this approach.     

Some remarks on the ionic conductivity in NaY dehydrated zeolite

On the basis of experimental measurements of the electrical conductivity of the Nafaujasite zeolites (NaY), treated under vacuum up to 673 K for 24 hours, we clearly demonstrate that the behavior of the measured conductivity σ_ac of the dehydrated zeolite NaY, over an interval of high frequency change, may be described by a power-law function: σ_ac=A▹^s. The exponent s, in this case, should be considered as temperature and frequency dependent when the parameter A is a temperature dependent function. On the other hand, when considering the measured conductivity as a sum of two terms (σ_ac=σ₀+σ′(▹)) resulting from the contributions of the dc and the ac components respectively, we find that one of them obeys the Arrhenius law while the other can be expressed as A▹^s. Parameter s is practically frequency independent when the frequency of the applied electrical field is higher than a characteristic value ▹_c A comparison with the measurements performed on NaY dehydrated at 435 K is also included. Paper presented at the 2nd Euroconference on Solid State Ionics, Funchal, Madeira, Portugal, Sept. 10–16, 1995     

Predicting the viscosity and electrical conductivity of ionic liquids on the basis of theoretically calculated ionic volumes

Selected physical properties of the ionic liquids might be quantitatively predicted based on the volumes of the ions these systems are composed of. It is demonstrated that the ionic volumes calculated using relatively simple theoretical quantum chemistry methods can be utilised to estimate the viscosities and electrical conductivities of various commonly used ionic liquids. The fitting formulas of the exponential form are offered and their predictive usefulness is verified. The quality of such predictions is discussed on the basis of several ionic liquids involving [Tf₂N]^? and [BF₄]^? anions and 16 various cations. The dependence of the viscosity and electrical conductivity of the ionic liquids on the temperature is also investigated and the temperature-dependent equations are derived and compared to the experimentally measured values.     

掺杂对铌酸锂晶体非挥发全息存储性能的影响

通过研究掺镁、掺锌和掺铟同成分铌酸锂晶体的紫外-红光双色全息存储性能,发现双色记录响应时间均比单色记录时明显缩短,最多的可减小3个数量级;双色记录灵敏度大幅度提高,在掺镁5 mol.%的晶体中可达到11 cm/J.在掺杂浓度超过抗光损伤阈值的铌酸锂晶体中,均可实现非挥发全息存储.但是,在掺镁、锌样品中,深、浅能级中心上的光栅反相,而在掺铟样品中则表现为同相.这是由于掺杂离子的种类不同,在铌酸锂晶体中形成的缺陷中心也不同所引起的. 关键词： 掺杂 铌酸锂晶体 非挥发 全息存储     

Giant magnetoresistance in an electrochemically synthesized regimented array of nickel quantum dots

Giant magnetoresistance (GMR) due toremotespin dependent scattering of electrons has been observed in an electrochemically synthesized structure consisting of a two-dimensional, quasi-periodic array of nickel dots (diameter ∼100 Å) overlayed with a thin copper layer. Current flows exclusively in the copper layer, but the electrons scatter from the magnetic moments on the remote, underlying nickel quantum dots. Since the scattering cross-section depends on the magnetization of the dots, the resistance of the structure can be altered with a magnetic field which then gives rise to the GMR. The magnetoresistance is about 3% of the zero-field resistance up to a magnetic flux density of 2 tesla at room temperature.     

The corrosion behaviour of polypyrrole coating synthesized in phenylphosphonic acid solution

Electrochemical synthesis of polypyrrole (PPy) film was achieved on mild steel (MS), in monomer containing 0.1 M phenylphosphonic acid solution. The synthesis was carried out using cyclic voltammetry technique. It was found that the electrode surface could only become completely passive, after a few successive cycles in solution of 0.1 M pyrrole + 0.1 M phenylphosphonic acid. Then, the thickness of polymer film was increased with help of successive cycles in a relatively narrower potential range. The corrosion performance of polymer coating was investigated in 3.5% NaCl solution, using electrochemical impedance spectroscopy (EIS) and anodic polarization curves. It was shown that the coating had high stability and low permeability, under such aggressive conditions. The EIS results also showed that the coating exhibited important anodic protection behaviour on mild steel. The percent protection efficiency value (E%) was found to be 98.4% and the percent total porosity value (P%) was determined to be 0.752%, after 96 h exposure time to corrosive solution.     

The effect of ionic liquids on the conductivity of electrospun polyacrylonitrile membranes

Adding conductive additives to electrospinning solutions has been proven to increase the conductivity of electrospun membranes. The aim of this study was to learn the effect of ionic liquids (ILs) on the polyacrylonitrile membranes conductivity. Three different ionic liquids were used with concentration to 10 wt%. The conductivity of the membranes increases from picoS range without using IL to microS range with adding IL. At concentration 8 wt% ILs the percolation threshold was observed with maximum conductivity of the electrospun membranes. The maximum conductivity was measured to be 2.39 μS/cm.     

基于熵的离子导体电导率公式推导

电导率是表示导体导电能力强弱的度量,离子导体的电导率可以通过平均漂移速度求得.文中通过对离子导体的分析,给出一种基于熵的新的推导方法.首先分析系统熵和环境熵的竞争关系,其次运用熵最大原理求出最概然电流,进而导出电导率公式.最后将基于熵的推导方法与漂移速度方法加以区别和对比,并推广到一般导体电导率公式的推导.